| Literature DB >> 36163376 |
Ying Liu1,2, Yiwen Li3, Chengcheng Du3, Shouxiang Kuang3, Xuehao Zhou3, Jinyu Zhang3, Xiang Ao4,3.
Abstract
Cancer is the second-leading disease-related cause of global mortality after cardiovascular disease. Despite significant advances in cancer therapeutic strategies, cancer remains one of the major obstacles to human life extension. Cancer pathogenesis is extremely complicated and not fully understood. Epithelial splicing regulatory proteins (ESRPs), including ESRP1 and ESRP2, belong to the heterogeneous nuclear ribonucleoprotein family of RNA-binding proteins and are crucial regulators of the alternative splicing of messenger RNAs (mRNAs). The expression and activity of ESRPs are modulated by various mechanisms, including post-translational modifications and non-coding RNAs. Although a growing body of evidence suggests that ESRP dysregulation is closely associated with cancer progression, the detailed mechanisms remain inconclusive. In this review, we summarize recent findings on the structures, functions, and regulatory mechanisms of ESRPs and focus on their underlying mechanisms in cancer progression. We also highlight the clinical implications of ESRPs as prognostic biomarkers and therapeutic targets in cancer treatment. The information reviewed herein could be extremely beneficial to the development of individualized therapeutic strategies for cancer patients.Entities:
Keywords: Biomarker; CSC; EMT; ESRPs; Therapeutic target
Year: 2022 PMID: 36163376 DOI: 10.1007/s00109-022-02257-5
Source DB: PubMed Journal: J Mol Med (Berl) ISSN: 0946-2716 Impact factor: 5.606